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Pacific Northwest Angelman Syndrome Foundation


The Angelman Syndrome Foundation’s mission is to advance the awareness and treatment of Angelman syndrome through education and information, research, and support for individuals with Angelman syndrome, their families and other concerned parties. We exist to give all of them a reason to smile, with the ultimate goal of finding a cure.

FAST is an all-volunteer organization of families and professionals dedicated to finding a cure for Angelman Syndrome and related disorders through the funding of an aggressive research agenda, education, and advocacy. The Foundation is committed to assisting individuals living with Angelman Syndrome to realize their full potential and quality of life.

Angelman Today online magazine is the first and only publication of it’s kind.  Our articles feature information that we hope will revolutionize the current care and standard of practice for the treatment and education of those affected by AS.

The Canadian Angelman Syndrome Society (CASS) is dedicated to educating parents and professionals about Angelman Syndrome by disseminating information and providing support for parents and caregivers of children with Angelman Syndrome










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